Sugi Yukiko, Markwald Roger R
Department of Cell Biology and Anatomy and Cardiovascular Developmental Biology Center, Medical University of South Carolina, 171 Ashley Avenue, Charleston, SC 29425, USA.
Dev Biol. 2003 Nov 1;263(1):35-49. doi: 10.1016/s0012-1606(03)00433-0.
We previously demonstrated that the initial emergence of endocardial precursor cells (endocardial angioblasts) occurred within the precardiac mesoderm and that the endodermal secretory products promoted delamination of cells from the precardiac mesoderm and expression of endothelial lineage markers [Dev. Biol. 175 (1996), 66]. In this study, we sought to extend our original study to the identification of candidate molecules derived from the endoderm that might have induced endocardial precursor cell formation. We have detected expression of transforming growth factors beta (TGFbeta) 2, 3, and 4 in anterior endoderm at Hamburger and Hamilton (H-H) stage 5 by RT-PCR. To address the role of growth factors known to be present in the endoderm, precardiac mesodermal explants were isolated from H-H stage 5 quail embryos and cultured on the surface of collagen gels with serum-free defined medium 199. Similar to the effect of explants cocultured with anterior endoderm, when cultured with TGFbetas 1-3 (3 ng/ml each), explants formed QH-1 (anti-quail endothelial marker)-positive mesenchymal cells, which invaded the gel and expressed the extracellular marker, cytotactin (tenascin). Another member of the TGFbeta superfamily, bone morphogenetic protein-2 (BMP-2; 100 ng/ml), did not induce QH-1-positive mesenchymal cell formation but promoted formation of an epithelial monolayer on the surface of the collagen gel; this monolayer did not express QH-1. Explants treated with vascular endothelial growth factor (VEGF(165), 100 ng/ml) also did not invade the gel but formed an epithelial-like outgrowth on the surface of the gel. However, this monolayer did express the QH-1 marker. Fibroblast growth factor-2 (FGF-2; 250 ng/ml)-treated explants expressed QH-1 and exhibited separation of the cells on the surface of the gel. Finally, a combination of TGFbetas and VEGF enhanced formation of QH-1-positive cord-like structures within the gel from mesenchyme that had previously invaded the gel. Luminization of the cords, however, was not clearly evident. These findings suggest that TGFbetas, among the growth factors tested, mediate the initial step of endocardial formation, i.e., delamination of endothelial precursor cells from precardiac mesoderm, whereas VEGF may primarily effect early vasculogenesis (cord-like structure formation).
我们之前证明,心内膜前体细胞(心内膜成血管细胞)最初出现在心脏前中胚层内,并且内胚层分泌产物促进细胞从心脏前中胚层分层以及内皮谱系标志物的表达[《发育生物学》175(1996),66]。在本研究中,我们试图将最初的研究扩展至鉴定可能诱导心内膜前体细胞形成的内胚层衍生候选分子。我们通过逆转录聚合酶链反应在汉伯格和汉密尔顿(H-H)第5阶段的前肠内胚层中检测到转化生长因子β(TGFβ)2、3和4的表达。为了探讨已知存在于内胚层中的生长因子的作用,从H-H第5阶段的鹌鹑胚胎中分离出心脏前中胚层外植体,并在含有无血清限定培养基199的胶原凝胶表面进行培养。与与前肠内胚层共培养的外植体的效果类似,当与TGFβ1-3(各3 ng/ml)一起培养时,外植体形成QH-1(抗鹌鹑内皮标志物)阳性间充质细胞,这些细胞侵入凝胶并表达细胞外标志物细胞结合素(腱生蛋白)。TGFβ超家族的另一个成员骨形态发生蛋白-2(BMP-2;100 ng/ml)未诱导QH-1阳性间充质细胞形成,但促进了胶原凝胶表面上皮单层的形成;该单层不表达QH-1。用血管内皮生长因子(VEGF(165),100 ng/ml)处理的外植体也未侵入凝胶,但在凝胶表面形成上皮样生长物。然而,该单层确实表达QH-1标志物。用成纤维细胞生长因子-2(FGF-(250 ng/ml)处理的外植体表达QH-1,并在凝胶表面出现细胞分离。最后,TGFβ和VEGF的组合增强了凝胶内先前侵入凝胶的间充质中QH-1阳性索状结构的形成。然而,索状结构的发光并不明显。这些发现表明,在所测试的生长因子中,TGFβ介导心内膜形成的初始步骤,即内皮前体细胞从心脏前中胚层分层,而VEGF可能主要影响早期血管生成(索状结构形成)。